Variant report

Variant rs35826019
Chromosome Location chr14:104654947-104654948
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104643800-104662200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr14:104645400-104655000 Weak transcription Gastric stomach
3 chr14:104648200-104655000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr14:104651600-104655000 Weak transcription Fetal Intestine Small intestine
5 chr14:104652400-104655800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr14:104652600-104660400 Weak transcription Spleen Spleen
7 chr14:104653400-104655400 Bivalent Enhancer Placenta Placenta
8 chr14:104653600-104655000 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
9 chr14:104653600-104656200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr14:104653800-104655000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr14:104653800-104655400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr14:104654000-104655000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr14:104654000-104655200 Bivalent Enhancer Fetal Muscle Leg muscle
14 chr14:104654200-104655000 Enhancers Rectal Mucosa Donor 29 rectum
15 chr14:104654400-104655200 Enhancers Brain Germinal Matrix brain
16 chr14:104654400-104655400 Bivalent Enhancer Fetal Muscle Trunk muscle
17 chr14:104654400-104655400 Enhancers Rectal Mucosa Donor 31 rectum
18 chr14:104654600-104655600 Bivalent Enhancer Stomach Mucosa stomach
19 chr14:104654800-104655000 Enhancers Fetal Brain Male brain

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